4.6 Article

Fundamental role for the KCNE4 ancillary subunit in Kv7.4 regulation of arterial tone

期刊

JOURNAL OF PHYSIOLOGY-LONDON
卷 593, 期 24, 页码 5325-5340

出版社

WILEY
DOI: 10.1113/JP271286

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资金

  1. European Union [608765]
  2. Lundbeck Foundation
  3. Medical Research Council [MR/K019074/1]
  4. Danish National Research Foundation
  5. MRC [MR/K019074/1] Funding Source: UKRI
  6. Lundbeck Foundation [R181-2014-4030] Funding Source: researchfish
  7. Medical Research Council [MR/K019074/1] Funding Source: researchfish
  8. Novo Nordisk Fonden [NNF13OC0006553] Funding Source: researchfish

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The KCNE ancillary subunits (KCNE1-5) significantly alter the expression and function of voltage-gated potassium channels; however, their role in the vasculature has yet to be determined. The present study aimed to investigate the expression and function of the KCNE4 subunit in rat mesenteric arteries and to determine whether it has a functional impact on the regulation of arterial tone by Kv7 channels. In HEK cells expressing Kv7.4, co-expression of KCNE4 increased the membrane expression of Kv7.4 and significantly altered Kv7.4 current properties. Quantitative PCR analysis of different rat arteries found that the KCNE4 isoform pre-dominated and proximity ligation experiments showed that KCNE4 co-localized with Kv7.4 in mesenteric arterymyocytes. Morpholino-induced knockdown of KCNE4 depolarized mesenteric artery smooth muscle cells and resulted in their increased sensitivity to methoxamine being attenuated (mean +/- SEM EC50 decreased from 5.7 +/- 0.63 mu M to 1.6 +/- 0.23 mu M), which coincided with impaired effects of Kv7 modulators. When KCNE4 expression was reduced, less Kv7.4 expression was found in the membrane of the mesenteric artery myocytes. These data show that KCNE4 is consistently expressed in a variety of arteries, and knockdown of the expression product leads to reduced Kv7.4 membrane abundance, a depolarized membrane potential and an augmented response to vasoconstrictors. The present study is the first to demonstrate an integral role of KCNE4 in regulating the function and expression of Kv7.4 in vascular smooth muscle.

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